Mixture of phosphanes and chromane derivatives

ABSTRACT

The invention relates to a synergistic mixture comprising
     a) at least one compound from the group which consists of the phosphanes of the formula (I), (di/oligo)phosphanes of the formulae (II) and (III) and cyclophosphanes of the formula (IV)
 
and
   b) at least one 6-hydroxychromane derivative of the general formula (V)
 
and also to a process which stabilizes polymers with respect to thermooxidative degradation by addition and incorporation of this synergistic mixture.

This application is a 371 of PCT/IB00/01897 filed Dec. 18, 2000.

The invention relates to synergistic mixtures which comprise phosphanes, (di/oligo)-phosphanes, cyclophosphanes as component 1 and 6-hydroxychromane derivatives as component 2, and also to a process which uses these mixtures to stabilize polymers with respect to degradation initiated by heat or by mechanical stress.

When polymers are processed to give the final products they are exposed, inter alia, to high temperatures. This can have adverse effects on the melt viscosity and physical properties of the polymers, and also on the appearance of the final products produced from them. Suitable stabilizers or stabilizer systems are therefore required in order to minimize oxidation, chain breakage or discoloration.

However, many of the known stabilizers or stabilizer systems have disadvantages, e.g. insufficient efficacy and shortcomings with respect to other requirements, e.g. inadequate stability with respect to hydrolysis, tendency to develop colour, very limited compatibility with the polymers to be stabilized and restricted thermal stability. Due to limited compatibility, it is desirable to have lower concentrations of these stabilizers in the polymers, this being achievable by using more efficacious stabilizer systems.

An object of the present patent application is therefore to provide novel stabilizer systems which give better performance.

This object is achieved by way of the synergistic stabilizer mixture of the invention, which is an improved processing stabilizer for polymers since even when used in small amounts it inhibits the damaging reactions caused by heat.

The invention provides a mixture comprising

-   a) at least one compound from the group of compounds of the     formulae (I) to (IV) [hereinafter termed component 1]

-    and -   b) at least one compound of the general formula (V) [hereinafter     termed component 2]

-    where, independently of one another, -   R₁ is C₁–C₂₄-alkyl (linear or branched), C₅–C₃₀-cycloalkyl     C₁–C₃₀-alkylaryl, C₆–C₂₄-aryl, C₄–C₂₄-heteroaryl, C₆–C₂₄-aryl or     C₄–C₂₄-heteroaryl (mono- or polysubstituted by the groups     C₁–C₁₈-alkyl (linear or branched)), C₅–C₁₂-cycloalkyl or     C₁–C₁₈-alkoxy; -   R₂ is C₄–C₂₄-alkyl (linear or branched), C₅–C₃₀-cycloalkyl,     C₁–C₃₀-alkylaryl, C₆–C₂₄-aryl, C₄–C₂₄-heteroaryl, C₆–C₂₄-aryl or     C₄–C₂₄-heteroaryl (mono- or polysubstituted by the groups     C₁–C₁₈-alkyl (linear or branched)), C₅–C₁₂-cycloalkyl or     C₁–C₁₈-alkoxy; -   R₃ is hydrogen, C₁–C₂₄-alkyl (linear or branched),     C₃–C₁₂-cycloalkyl, C₁–C₂₄-alkenyl (mono- or polyunsaturated, linear     or branched); -   R₄, R₅, R₆, R₇ are hydrogen, C₁–C₂₄-alkyl (linear or branched),     C₃–C₁₂-cycloalkyl, C₁–C₂₄-alkenyl (mono- or polyunsaturated, linear     or branched), carboxy groups —COOR₈, succinyl groups     —CH(COOR₈)—CH₂—COOR₈; -   R₈ is hydrogen, C₁–C₂₀-alkyl (linear or branched), C₄–C₁₂-cycloalkyl     or C₂–C₂₀-polyethylene glycol groups; -   D is C₁–C₃₀-alkylene (linear or branched), C₂–C₃₀-alkylidene     C₅–C₁₂-cyclo-alkylene or C₆–C₂₄-arylene or C₄–C₂₄-heteroarylene,     C₆–C₂₄-arylene or C₄–C₂₄-heteroarylene (mono- or polysubstituted by     C₁–C₁₈-alkyl (linear or branched)), C₅–C₁₂-cycloalkyl or     C₁–C₁₈-alkoxy; -   q is from 1 to 5; -   r is from 3 to 6, the groups P-R₁ in the formula (IV) being a     constituent of a phosphacycle indicated by * on the bonds emanating     from P.

Preference is given to mixtures in which the radicals R and the alphabetical characters in the formulae relating to compounds (I) to (V) have the following meanings:

-   R₁′ is C₈–C₂₄-alkyl (linear or branched), C₆–C₁₂-cycloalkyl,     C₂–C₂₄-alkylaryl, C₆–C₂₄-aryl or C₄–C₁₈-heteroaryl, C₆–C₂₄-aryl or     heteroaryl (mono- or polysubstituted by the groups C₁–C₁₂-alkyl     (linear or branched)), C₅–C₈-cycloalkyl or C₁–C₁₂-alkoxy; -   R₂′ is C₆–C₁₈-alkyl (linear or branched), C₅–C₁₂-cycloalkyl     C₁–C₁₈-alkylaryl, C₆–C₂₄-aryl, C₄–C₁₈-heteroaryl, C₆–C₂₄-aryl or     C₄–C₁₈-heteroaryl (mono- or polysubstituted by the groups     C₁–C₁₂-alkyl (linear or branched)), C₅–C₈-cycloalkyl or     C₁–C₁₂-alkoxy; -   R₃′ is C₁–C₂₀-alkyl (linear or branched), C₄–C₈-cycloalkyl,     C₁–C₂₀-alkenyl (mono- or polyunsaturated, linear or branched); -   R₄′, R₅′, R₆′, R₇′ are hydrogen, C₁–C₂₀-alkyl (linear or branched),     C₄–C₈-cycloalkyl, C₁–C₂₀-alkenyl (mono- or polyunsaturated, linear     or branched), carboxy groups, —COOR₈′, succinyl groups     —CH(COOR₈′)—CH₂—COOR₈′; -   R₈′ is hydrogen, C₁–C₁₂-alkyl (linear or branched), C₄–C₈-cycloalkyl     or C₄–C₁₆-polyethylene glycol groups; -   D′ is C₁–C₂₄-alkylene (linear or branched), C₂–C₂₄-alkylidene,     C₅–C₈-cyclo-alkylene, or C₆–C₂₄-arylene or C₄–C₁₈-heteroarylene,     C₆–C₂₄-arylene or C₄–C₁₈-heteroarylene (mono- or polysubstituted by     C₁–C₁₈-alkyl (linear or branched)), C₅–C₈-cycloalkyl or     C₁–C₁₂-alkoxy; -   q′ is from 1 to 4; -   r′ is from 4 to 5, the groups P—R₁ in the formula (IV) being a     constituent of a phosphacycle indicated by * on the bonds emanating     from P.

Particular preference is given to mixtures in which the radicals R and the alphabetic characters in the formulae relating to compounds (I) to (V) have the following meanings:

-   R₁″ is C₆–C₂₄-aryl or C₄–C₁₈-heteroaryl, C₆–C₂₄-aryl or     C₄–C₁₈-heteroaryl (mono- or polysubstituted by the groups     C₁–C₁₂-alkyl (linear or branched)), C₅–C₈-cycloalkyl or     C₁–C₁₂-alkoxy; -   R₂″ is C₈–C₁₈-alkyl (linear or branched), C₅–C₈-cycloalkyl,     C₁–C₁₈-alkylaryl, C₆–C₁₂-aryl, C₄–C₁₈-heteroaryl, C₆–C₁₂-aryl or     C₄–C₁₈-heteroaryl (mono- or polysubstituted by the groups     C₁–C₁₂-alkyl (linear or branched)), C₆–C₈-cycloalkyl or     C₁–C₈-alkoxy; -   R₃″ is C₁–C₁₆-alkyl (linear or branched), C₅–C₈-cycloalkyl,     C₁–C₁₆-alkenyl (mono- or polyunsaturated, linear or branched); -   R₄″, R₅″, R₆″, R₇″ are hydrogen, C₁–C₁₆-alkyl (linear or branched),     C₅–C₈-cycloalkyl, C₁–C₁₆-alkenyl (mono- or polyunsaturated, linear     or branched); —COOR₈″, —CH(COOR₈″)—CH₂—COOR₈″; -   R₈″ is hydrogen, C₁–C₈-alkyl (linear or branched), C₅–C₈-cycloalkyl     or C₆–C₁₂-polyethylene glycol groups; -   D″ is C₁–C₁₈-alkylene (linear or branched), C₂–C₂₄-alkylidene,     C₅–C₈-cyclo-alkylene, or C₆–C₂₄-arylene or C₄–C₁₈-heteroarylene,     C₆–C₂₄-arylene or C₄–C₁₈-heteroarylene (mono- or polysubstituted by     C₁–C₁₈-alkyl (linear or branched)), C₅–C₈-cycloalkyl or     C₁–C₁₂-alkoxy; -   q″ is from 1 to 4; -   r″ is from 4 to 5, the groups P-R₁ in the formula (IV) being a     constituent of a phosphacycle indicated by * on the bonds emanating     from P.

Particularly suitable mixtures are all of those which can be formed by combining one or more of the components 1 and 2 mentioned below:

Component 1 triphenylphosphane tris(2-methylphenyl)phosphane tris(4-methylphenyl)phosphane tris(2-methoxyphenyl)phosphane tris(4-methoxyphenyl)phosphane tetracyclohexylcyclotetraphosphane tetra-tert-butylcyclotetraphosphane tetrabiphenylylcyclotetraphosphane tetraphenylcyclotetraphosphane pentaphenylcyclopentaphosphane pentabiphenylylcyclopentaphosphane tetraphenyldiphosphane tetracyclohexyldiphosphane bis(diphenylphosphino)methane 1,2-bis(diphenylphosphino)ethane 1,3-bis(diphenylphosphino)propane 1,4-bis(diphenylphosphino)butane 1,5-bis(diphenylphosphino)pentane 1,6-bis(diphenylphosphino)hexane 1,8-bis(diphenylphosphino)octane 1,3-bis(diphenylphosphino)-2,2-dimethylpropane 1,1,1-tris(diphenylphosphinomethyl)methane 1,1,1-tris(diphenylphosphinomethyl)ethane 1,1,1-tris(diphenylphosphinomethyl)propane 1,1,1-tris(diphenylphosphinomethyl)butane 1,1,1-tris(diphenylphosphinomethyl)-1-phenylmethane 1,3-bis(diphenylphosphinomethyl)-2,2-diphenylphosphinopropane 1,3-bis(diphenylphosphinomethyl)-2,2-diethylphosphinopropane 1,3-bis(diphenylphosphino)-2-methylpropane Component 2 2,5,7,8-tetramethyl-2-(4′,8′,12′-trimethyltridecyl)chroman-6-ol (α- tocopherol) 2,5,8-trimethyl-2-(4′,8′,12′-trimethyltridecyl)chroman-6-ol (β-tocopherol) 2,7,8-trimethyl-2-(4′,8′,12′-trimethyltridecyl)chroman-6-ol (γ-tocopherol) 2,8-dimethyl-2-(4′,8′,12′-trimethyltridecyl)chroman-6-ol (δ-tocopherol) 3,4-dihydro-2,2,5,7,8-pentamethyl-2H-1-benzopyran-6-ol 6-hydroxy-2,5,7,8-tetramethylchromane-2-carboxylic acid (Trolox)

Among these mixtures, very particular preference is given to the following mixtures of components 1 and 2:

-   A) where component 1 is triphenylphosphane and component 2 is     α-tocopherol; -   B) where component 1 is triphenylphosphane and component 2 is     3,4-dihydro-2,2,5,7,8-pentamethyl-2H-1-benzopyran-6-ol; -   C) where component 1 is tris(4-methylphenyl)phosphane and component     2 is α-tocopherol; -   D) where component 1 is tris(4-methylphenyl)phosphane and component     2 is 3,4-dihydro-2,2,5,7,8-pentamethyl-2H-1-benzopyran-6-ol; -   E) where component 1 is tris(4-methoxyphenyl)phosphane and component     2 is α-tocopherol; -   F) where component 1 is tris(4-methoxyphenyl)phosphane and component     2 is 3,4-dihydro-2,2,5,7,8-pentamethyl-2H-1-benzopyran-6-ol; -   G) where component 1 is tris(2-methylphenyl)phosphane and component     2 is α-tocopherol; -   H) where component 1 is tris(2-methylphenyl)phosphane and component     2 is 3,4-dihydro-2,2,5,7,8-pentamethyl-2H-1-benzopyran-6-ol; -   I) where component 1 is tris(2-methoxyphenyl)phosphane and component     2 is α-tocopherol; -   J) where component 1 is tris(2-methoxyphenyl)phosphane and component     2 is 3,4-dihydro-2,2,5,7,8-pentamethyl-2H-1-benzopyran-6-ol; -   K) where component 1 is tetracyclohexylcyclotetraphosphane and     component 2 is α-tocopherol, -   L) where component 1 is tetracyclohexylcyclotetraphosphane and     component 2 is     3,4-dihydro-2,2,5,7,8-pentamethyl-2H-1-benzopyran-6-ol; -   M) where component 1 is bis(diphenylphosphino)methane and component     2 is α-toco-pherol; -   N) where component 1 is bis(diphenylphosphino)methane and component     2 is 3,4-dihydro-2,2,5,7,8-pentamethyl-2H-1-benzopyran-6-ol; -   O) where component 1 is 1,3-bis(diphenylphosphino)propane and     component 2 is α-tocopherol; -   P) where component 1 is 1,3-bis(diphenylphosphino)propane and     component 2 is     3,4-dihydro-2,2,5,7,8-pentamethyl-2H-1-benzopyran-6-ol; -   Q) where component 1 is     1,3-bis(diphenylphosphino)-2,2-dimethylpropane and component 2 is     α-tocopherol; -   R) where component 1 is     1,3-bis(diphenylphosphino)-2,2-dimethylpropane and component 2 is     3,4-dihydro-2,2,5,7,8-pentamethyl-2H-1-benzopyran-6-ol; -   S) where component 1 is 1,1,1-tris(diphenylphosphinomethyl)ethane     and component 2 is α-tocopherol; -   T) where component 1 is 1,1,1-tris(diphenylphosphinomethyl)ethane     and component 2 is 3,4-dihydro-2,2,5,7,     8-pentamethyl-2H-1-benzopyran-6-ol; -   U) where component 1 is 1,1,1-tris(diphenylphosphinomethyl)propane     and component 2 is α-tocopherol; -   V) where component 1 is 1,1,1-tris(diphenylphosphinomethyl)propane     and component 2 is     3,4-dihydro-2,2,5,7,8-pentamethyl-2H-1-benzopyran-6-ol.

Known mixtures based on commercially available stabilizers (phosphites/phosphonites) cannot achieve sufficient stabilization. In contrast, it is possible to use very small amounts of the components of the mixtures of the invention, sometimes less than 0.01% by weight, based on the polymeric material. Producers and users of these stabilized polymers can achieve an advantage in both economic and environmental terms through these markedly reduced usage concentrations of stabilizers.

Depending on the requirements profile placed upon the final products and the nature of the polymers to be stabilized, ideal stabilization can be achieved by varying the ratio of the two components.

The quantitative proportions of component 1 to component 2 in the mixture of the invention are preferably in the range from 50:1 to 2:1, with preference from 20:1 to 15:1, particularly preferably from 15:1 to 1:1.

Each of the components 1 and 2 may be composed either of one or of two or more compounds of the same component group.

Based on the polymeric material to be stabilized, the amounts used of the mixtures of components 1 and 2 are from 0.001 to 2% by weight, preferably from 0.005 to 1% by weight, particularly preferably from 0.0075 to 0.75% by weight.

Mixtures of components 1 and 2 may be prepared by simple mixing, by mixing in the melt, by dissolving or dispersing one component in the other liquid or molten component, by mixing two melts or by melting the materials together, where necessary, with a subsequent cooling step in each case. Mixtures of the invention are likewise obtained by mixing solutions of the components in suitable solvents and concentrating these by evaporation. The mixtures may be prepared either by a batch process in suitable apparatus, e.g. various mixers or reactors, etc., or else continuously, e.g. in extruders, continuous mixers, kneaders or roll mills. A suitable commercial form may then be prepared—if this further process is necessary—by compacting, pelletization, pressing, extrusion, or some other method.

The invention also provides a process which stabilizes polymeric materials with respect to thermooxidative degradation. This process encompasses the addition and incorporation of a stabilizing amount of the mixture of the invention in solid or molten form, in solution (preferably as liquid concentrate), in a mixture with other additives in the form of powder blends, in extrudates or in other commercial forms, as a compounded material (mixture of a polymer with a mixture of the invention and other additives, e.g. acid scavengers (e.g. metal soaps, dihydrotalcites, etc.), or with sterically hindered phenols, in the form of powder blends, extrudates or other commercial forms) or else as a solid masterbatch composition in amounts which achieve a stabilizer concentration of from 0.001 to 2% by weight, preferably from 0.005 to 1% by weight, particularly preferably from 0.0075 to 0.75% by weight, based on the polymeric material to be stabilized.

A liquid concentrate here encompasses from 10 to 80% by weight of a mixture of the invention and from 90 to 20% by weight of a solvent.

A masterbatch composition here (also termed solid base-compound) encompasses from 5 to 80% by weight, preferably from 10 to 70% by weight, particularly preferably from 15 to 40% by weight, of a mixture of the invention and from 95 to 20% by weight, preferably from 90 to 30% by weight, particularly preferably from 85 to 60% by weight, of a polymeric material which is identical or compatible with the polymeric material to be stabilized. The weights of the mixture of the invention present in a corresponding compounded material are the same as those in a masterbatch composition, but there is a reduction in the weight of the polymeric material corresponding to the amount of the other additives.

All of the components of the mixture of the invention may be prepared from known compounds using known methods.

The mixtures of the invention made from components 1 and 2 may be used as processing stabilizers for polymeric materials, preferably for

-   1. polymers of mono- and diolefins, e.g. polypropylene,     polyisobutylene, poly-1-butene, poly-4-methyl-1-pentene,     polyisoprene or polybutadiene, and also polymers of cycloolefins,     e.g. of cyclopentene or norbornene; also polyethylene (where     appropriate crosslinked), e.g. high-density polyethylene (HDPE),     low-density polyethylene (LDPE), linear low-density polyethylene     (LLDPE), branched low-density polyethylene (VLDPE) Polyolefins, i.e.     polymers of monoolefins, in particular polyethylene and     polypropylene, may be prepared by various processes, in particular     using the following methods:     -   a) free-radical polymerization (normally under high pressure and         at elevated temperature)     -   b) catalytic polymerization using a catalyst that normally         contains one or more metals of group IVb, Vb, VIb or VIII of the         Periodic Table. These metals usually have one or more ligands,         such as oxides, halides, alcoholates, esters, ethers, amines,         alkyls, alkenyls and/or aryls that may be either π- or         σ-coordinated. These metal complexes may be in the free form or         fixed on substrates, for example on activated magnesium         chloride, titanium chloride, alumina or silicon oxide. These         catalysts may be soluble or insoluble in the polymerization         medium The catalysts can be active as such in the polymerization         or further activators may be used, for example metal alkyls,         metal hydrides, metal alkyl halides, metal alkyl oxides or metal         alkyloxanes, the metals being elements of groups Ia, IIa and/or         IIIa of the Periodic Table. The activators may be modified, for         example, with further ester, ether, amine or silyl ether groups.         These catalyst systems are usually termed Phillips, Standard Oil         Indiana, Ziegler (-Natta), TNZ (DuPont), metallocene or single         site catalysts (SSC). -   2. Mixtures of the polymers mentioned under 1), e.g. mixtures of     polypropylene with polyisobutylene, polypropylene with polyethylene     (e.g. PP/HDPE, PP/LDPE, PP/LLDPE) and mixtures of various grades of     polyethylene (e.g. LDPE/HDPE). -   3. Copolymers of monoolefins and diolefins with each other or with     other vinyl monomers, for example ethylene-propylene copolymers,     linear low-density polyethylene (LLDPE) and mixtures thereof with     low-density polyethylene (LDPE), propylene-but-1-ene copolymers,     propylene-isobutylene copolymers, ethylene-but-1-ene copolymers,     ethylene-hexene copolymers, ethylene-methylpentene copolymers,     ethylene-heptene copolymers, ethylene-octene copolymers,     propylene-butadiene copolymers, isobutylene and isoprene copolymers,     ethylene-alkyl acrylate copolymers, ethylene-alkyl methacrylate     copolymers, ethylene-vinyl acetate copolymers and their copolymers     with carbon monoxide, or ethylene-acrylic acid copolymers and their     salts (ionomers) as well as terpolymers of ethylene with propylene     and a diene such as hexadiene, dicyclopentadiene or     ethylidene-norbornene; and mixtures of such copolymers with one     another and with polymers mentioned under 1), for example     polypropylene-ethylene-propylene copolymers, LDPE-ethylene-vinyl     acetate copolymers, LDPE-ethylene-acrylic acid copolymers,     LLDPE-ethylene-vinyl acetate copolymers, LLDPE-ethylene-acrylic acid     copolymers and alternating or random polyalkylene-carbon monoxide     copolymers and mixtures thereof with other polymers, for example     polyamides. -   4. Hydrocarbon resins (for example C₅–C₉) including hydrogenated     modifications thereof (e.g. tackifier resins) and mixtures of     polyalkylenes and starch. -   5. Polystyrene, poly(p-methylstyrene), poly(α-methylstyrene). -   6. Copolymers of styrene or α-methylstyrene with dienes or acrylic     derivatives, for example styrene-butadiene, styrene-acrylonitrile,     styrene-alkyl methacrylate, styrene-butadiene-alkyl acrylate,     styrene-butadiene-alkyl methacrylate, styrene-maleic anhydride,     styrene-acrylonitrile-methyl acrylate; mixtures of high impact     strength of styrene copolymers and another polymer, for example a     polyacrylate, a diene polymer or an ethylene-propylene-diene     terpolymer; and block copolymers of styrene, such as     styrene-butadiene-styrene, styrene-isoprene-styrene,     styrene-ethylene/butylene-styrene or     styrene-ethylene/propylene-styrene. -   7. Graft copolymers of styrene or α-methylstyrene, for example     styrene on polybutadiene, styrene on polybutadiene-styrene or     polybutadiene-acrylonitrile copolymers, styrene and acrylonitrile     (or methacrylonitrile) on polybutadiene; styrene, acrylonitrile and     methyl methacrylate on polybutadiene; styrene and maleic anhydride     on polybutadiene; styrene, acrylonitrile and maleic anhydride or     maleimide on polybutadiene; styrene and maleimide on polybutadiene;     styrene and alkyl acrylates or alkyl methacrylates on polybutadiene,     styrene and acrylonitrile on ethylene-propylene-diene terpolymers,     styrene and acrylonitrile on polyalkyl acrylates or polyalkyl     methacrylates, styrene and acrylonitrile on acrylate-butadiene     copolymers, as well as mixtures thereof with the copolymers     mentioned under 6), for example the copolymer mixtures known as ABS,     MBS, ASA or AES polymers. -   8. Halogen-containing polymers, such as polychloroprene, chlorinated     rubber, chlorinated or sulphochlorinated polyethylene, copolymers of     ethylene and chlorinated ethylene, epichlorohydrin homo- and     copolymers, especially polymers of halogen-containing vinyl     compounds, for example polyvinyl chloride, polyvinylidene chloride,     polyvinyl fluoride, polyvinylidene fluoride; as well as copolymers     thereof such as vinyl chloride-vinylidene chloride, vinyl     chloride-vinyl acetate or vinylidene chloride-vinyl acetate. -   9. Polymers derived from α,α-unsaturated acids and derivatives     thereof, such as polyacrylates and polymethacrylates,     polyacrylonitriles, polyacrylamides and polymethyl methacrylates     impact-modified with butyl acrylate. -   10. Copolymers of the monomers mentioned under 9) with each other or     with other unsaturated monomers, for example acrylonitrile-butadiene     copolymers, acrylonitrile-alkyl acrylate copolymers,     acrylonitrile-alkoxyalkyl acrylate copolymers, acrylonitrile-vinyl     halide copolymers or acrylonitrile-alkyl methacrylate-butadiene     terpolymers. -   11. Polymers derived from unsaturated alcohols and amines or the     acyl derivatives or acetals thereof, such as polyvinyl alcohol,     polyvinyl acetate, polyvinyl stearate, polyvinyl benzoate, polyvinyl     maleate, polyvinyl butyral, polyallyl phthalate or polyallyl     melamine; as well as their copolymers with olefins mentioned in     section 1. -   12. Homopolymers and copolymers of cyclic ethers, such as     polyalkylene glycols, polyethylene oxide, polypropylene oxide or     copolymers thereof with bisglycidyl ethers. -   13. Polyacetals such as polyoxymethylene and those polyoxymethylenes     which contain comonomers, for example ethylene oxide; polyacetals     modified with thermoplastic polyurethanes, acrylates or MBS. -   14. Polyphenylene oxides and sulphides, and mixtures thereof with     styrene polymers or polyamides. -   15. Polyurethanes derived from hydroxyl-terminated polyethers,     polyesters and polybutadienes on the one hand and aliphatic or     aromatic polyisocyanates on the other, as well as precursors     thereof. -   16. Polyamides and copolyamides derived from diamines and     dicarboxylic acids and/or from aminocarboxylic acids or the     corresponding lactams, such as polyamide 4, 6, 6/6, 6/10, 6/9, 6/12,     4/6, 12/12, 11 and 12, aromatic polyamides starting from m-xylene,     diamine and adipic acid; polyamides prepared from     hexamethylenediamine and isophthalic and/or terephthalic acid and     with or without an elastomer as modifier, for example     poly-2,4,4-trimethylhexamethylene terephthalamide or     poly-m-phenylene isophthalamide, block copolymers of the     aforementioned polyamides with polyolefins, olefin copolymers,     ionomers or chemically bonded or grafted elastomers; or with     polyethers, e.g. with polyethylene glycol, polypropylene glycol or     polytetramethylene glycol. As well as polyamides or copolyamides     modified with EPDM or ABS; and polyamides condensed during     processing (RIM polyamide systems). -   17. Polyureas, polyimides, polyamide-imides and polybenzimidazoles. -   18. Polyesters derived from dicarboxylic acids and dialcohols and/or     from hydroxycarboxylic acids or the corresponding lactones, such as     polyethylene terephthalate, polybutylene terephthalate,     poly-1,4-dimethylolcyclohexane terephthalate, polyhydroxybenzoates,     as well as block polyether-esters derived from hydroxyl-terminated     polyethers; and also polyesters modified with polycarbonates or MBS. -   19. Polycarbonates and polyester carbonates. -   20. Polysulphones, polyether sulphones and polyether ketones. -   21. Crosslinked polymers derived from aldehydes on the one hand and     phenols, urea or melamine on the other hand, such as     phenol/formaldehyde resins, urea/formaldehyde resins and     melamine/formaldehyde resins. -   22. Drying and non-drying alkyd resins. -   23. Unsaturated polyester resins derived from copolyesters of     saturated and unsaturated dicarboxylic acids with polyhydric     alcohols and vinyl compounds as crosslinking agents, and also     halogen-containing modifications thereof of low flammability. -   24. Crosslinkable acrylic resins derived from substituted acrylates,     for example from epoxy acrylates, urethane acrylates or polyester     acrylates. -   25. Alkyd resins, polyester resins and acrylic resins crosslinked     with melamine resins, urea resins, polyisocyanates or epoxy resins. -   26. Crosslinked epoxy resins which derive from polyepoxides, e.g.     from bis-glycidyl ethers or from cycloaliphatic diepoxides. -   27. Natural polymers such as cellulose, natural rubber, gelatin and     derivatives thereof which have been chemically modified in a     polymer-homologous manner, for example cellulose acetates, cellulose     propionates and cellulose butyrates, or the cellulose ethers such as     methyl cellulose; as well as rosins and derivatives. -   28. Mixtures (polyblends) of the aforementioned polymers, for     example PP/EPDM, polyamide/EPDM or ABS, PVC/EVA, PVC/ABS, PVC/MBS,     PC/ABS, PBTP/ABS, PC/ASA, PC/PBT, PVC/CPE, PVC/acrylates,     POM/thermoplastic PUR, PC/thermoplastic PUR, POM/acrylate, POM/MBS,     PPO/HIPS, PPO/PA 6.6 and copolymers, PA/PE-HD, PA/PP, PA/PPO. -   29. Natural and synthetic organic substances which constitute pure     monomeric compounds or mixtures thereof, examples being mineral     oils, animal or vegetable fats, oils and waxes, or oils, waxes and     fats based on synthetic esters (e.g. phthalates, adipates,     phosphates or trimellitates), and also blends of synthetic esters     with mineral oils in any desired proportion by weight, as are     employed, for example, as spin finishes, and aqueous emulsions     thereof. -   30. Aqueous emulsions of natural or synthetic rubbers, such as     natural rubber latex or latices of carboxylated styrene-butadiene     copolymers.

Particularly preferred polymers to be stabilized are polyolefins, polyurethanes and polycarbonates

These polymers may comprise other additives, e.g. antioxidants, light stabilizers (UV absorbers and/or HALS compounds and/or UV quenchers), metal deactivators, peroxide degraders, polyamide stabilizers, basic co-stabilizers, nucleating agents, fillers, reinforcing agents, plasticizers, lubricants, emulsifiers, pigments and dyes, optical brighteners, flame retardants, antistats, blowing agents, peroxides, hydroxylamines, polyalcohols, nitrones, colour improvers, thiosynergists, rheology additives, dispersing agents, etc.

These further additives may be added to the polymers prior to, together with or after the addition of the mixture of the invention. The feed here of these additives, and also of the mixture of the invention, may be in the form of a solid, or a solution or melt, or else in the form of solid or liquid mixtures or masterbatches/concentrates, using batch operation or else continuously.

The invention also encompasses all of the products obtainable by moulding the abovementioned polymers which comprise a mixture of the invention and comprise at least one of the abovementioned other additives.

The advantageous action of the mixture of the invention is illustrated by the examples below

EXAMPLE 1

To prepare a polymer stabilized according to the invention,

100.00 parts of polypropylene (Eltex P HL 001PF, Solvay) 0.05 part of Hostanox O-10 (sterically hindered phenol, Clariant AG) 0.10 part of calcium stearate and 0.04 part of 1,3-bis(diphenylphosphino)-2,2-dimethylpropane (component 1) and 0.01 part of α-tocopherol (Ronotec 201, Hoffman-La Roche) (component 2) are mixed in a Kenwood mixer and then homogenized by non-aggressive extrusion in a single-screw extruder (Collin, 210° C., 80 rpm, compression ratio 1:3, die 4 mm), and the resultant polymer extrudate is pelletized. To study melt flow stabilization and colour stabilization, the stabilized polymers are extruded five times at 270° C. in a single-screw extruder (Göttfert Extrusiometer, 50 rpm, compression ratio 1:3, die 2 mm). After the 5th pass the melt flow index (MFI) is determined to ASTM 1238 cond. L (230° C./2.16 kg)

EXAMPLE 2

Using a method similar to that of Example 1, another stabilized polymer of the invention is prepared from

100.00 parts of polypropylene (Eltex P HL 001PF, Solvay) 0.05 part of Hostanox O-10 (sterically hindered phenol, Clariant AG) 0.10 part of calcium stearate and 0.04 part of 1,1,1-tris(diphenylphosphinomethyl)ethane (component 1) and 0.01 part of α-tocopherol (Ronotec 201, Hoffman-La Roche) (component 2).

EXAMPLE 3

Using a method similar to that of Example 1, another stabilized polymer of the invention is prepared from

100.00 parts of polypropylene (Eltex P HL001 PF, Solvay) 0.05 part of Hostanox O-10 (sterically hindered phenol, Clariant AG) 0.10 part of calcium stearate and 0.04 part of 1,1,1-tris(diphenylphosphinomethyl)propane (component 1) and 0.01 part of α-tocopherol (Ronotec 201, Hoffman-La Roche) (component 2).

The following comparative mixtures are prepared:

EXAMPLE 4 Comparative Mixture Without Component 1

Using a method based on Example 1, a polymer stabilized according to the prior art is prepared for comparative purposes from

100.00 parts of polypropylene (Eltex P HL 001PF, Solvay) 0.05 part of Hostanox O-10 (sterically hindered phenol, Clariant AG) 0.10 part of calcium stearate and 0.05 part of α-tocopherol (Ronotec 201, Hoffman-La Roche).

EXAMPLE 5 Comparative Mixture Without Component 2

Using a method based on Example 1, a polymer stabilized according to the prior art is prepared for comparative purposes from

100.00 parts of polypropylene (Eltex P HL 001PF, Solvay) 0.05 part of Hostanox O-10 (sterically hindered phenol, Clariant AG) 0.10 part of calcium stearate and 0.05 part of 1,3-bis(diphenylphosphino)-2,2-dimethylpropane.

EXAMPLE 6 Comparative Mixture Without Component 2

Using a method based on Example 1, a polymer stabilized according to the prior art is prepared for comparative purposes from

100.00 parts of polypropylene (Eltex P HL 001PF, Solvay) 0.05 part of Hostanox O-10 (sterically hindered phenol, Clariant AG) 0.10 part of calcium stearate and 0.05 part of 1,1,1-tris(diphenylphosphinomethyl)ethane.

EXAMPLE 7 Comparative Mixture Without Component 2

Using a method based on Example 1, a polymer stabilized according to the prior art is prepared for comparative purposes from

100.00 parts of polypropylene (Eltex P HL 001PF, Solvay) 0.05 part of Hostanox O-10 (sterically hindered phenol, Clariant AG) 0.10 part of calcium stearate and 0.05 part of 1,1,1-tris(diphenylphosphinomethyl)propane.

The results obtained are given in the table below.

TABLE 1 Results of melt flow stabilization measurements on a polypropylene stabilized with 0.05 part of stabilizer (mixture). Melt Flow Index (230° C., 2.16 kg) [g/10 min] Example 5th pass 1 4.43 2 3.41 3 3.39 4 6.41 5 4.60 6 4.02 7 3.99

The results show that when a prior art stabilizer (Ronotec 201, Example 4; component 2) which is in itself a relatively poor stabilizer is added to another prior art stabilizer (Examples 5–7; component 1) the result is synergistic mixtures of the invention (Examples 1–3) with improved stabilization properties (corresponding to lower MFI values due to reduced degradation of the polypropylene chain). This is surprising, since if the change in stabilizing action were additive and therefore linear the activity of mixtures of components 1 and 2 would have been expected to be poorer than that of pure component 1 (Examples 5–7). 

1. Mixture comprising a) a compound of formula (II) [hereinafter termed component 1]

 and b) at least one compound of the general formula (V) [hereinafter termed component 2]


2. Mixture according to claim 1, where the quantitative ratio of formula (II) to formula (V) is from 50:1 to 2:1.
 3. Mixture according to claim 1, where the quantitative ratio of formula (II) to formula (V) is from 20:1 to 1.5:1.
 4. Mixture according to claim 1, where the quantitative ratio of formula (II) to formula (V) is from 15:1 to 1:1.
 5. A composition comprising: at least one polymeric material; and a mixture according to claim
 1. 